Empagliflozin 10 MG
DrugPatient will be given 10 mg of Empagliflozin if randomized to the drug arm or will receive placebo drug for 1 year
Other names: Jardiance, Empagliflozin
NCT Number: NCT06260059
The goal of the study is to investigate the feasibility and benefit of novel guideline-directed heart failure therapy drug Empagliflozin (Jardiance) for adult patients with congenital heart disease (ACHD).
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 4
Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United States
As CHD adolescents transition to adulthood, it is becoming evident that in addition to their structural cardiac abnormalities, they also have an intrinsic disease of the heart muscle which manifests as abnormal heart rhythm (arrhythmia) and decreased function (heart failure).
The lifesaving cardiac surgeries during childhood can also contribute to this dysfunction (cardiomyopathy). Hence, patients with CHD require multiple interventions and close clinical follow-up throughout their life. Currently, there are over 2.5 million CHD patients in the U.S. alone, and an additional 40,000 babies are born with CHD every year. Up to 50% of these patients require inpatient hospital care at some point due to their cardiomyopathy.
High-risk ACHD patients do not receive treatment until they present with heart failure or arrhythmia, at which time there is significant evidence of myocardial disease and dysfunction.
Empagliflozin (Jardiance) is an FDA-approved drug that significantly reduces hospitalization risk and cardiovascular death in adult patients with non-CHD heart failure. Studies show that Empagliflozin protects the heart from inflammation, and preliminary evaluation of Empagliflozin in symptomatic ACHD patients showed improved cardiac function and a reduction in heart failure including decreased shortness of breath and increased functional capacity. Empagliflozin as a preventative therapy may delay the onset of comorbidities by reducing inflammation in ACHD patients.
The study hypothesis is that the administration of once-a-day oral Jardiance (Empagliflozin) medication for one year reduces arrhythmia and cardiomyopathy and lowers serum circulating inflammatory factors and improves neurocognitive outcomes in susceptible ACHD patients.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patient will be given 10 mg of Empagliflozin if randomized to the drug arm or will receive placebo drug for 1 year
Other names: Jardiance, Empagliflozin
To patients randomized to the placebo group, a placebo pill will be given
Other names: Placebo Drug
Time frame: Change from baseline in ejection fraction at 1-year
Cardiac Magnetic Resonance Imaging (cMRI) and echocardiography will be used to measure ventricular function
Time frame: Change from baseline in T1 mapping at 1-year
Cardiac Magnetic Resonance Imaging (cMRI) without contrast will be used to measure myocardial characteristics
Time frame: Change from baseline of global strain on MRI at 1 year
Cardiac Magnetic Resonance Imaging (cMRI) will be used to measure myocardial characteristics
Time frame: Change from baseline of global strain on echocardiogram at 1 year
Echocardiography will be used to measure myocardial characteristics such as global longitudinal strain
Time frame: Change from baseline of exercise capacity at 1-year
Cardiopulmonary exercise stress testing (CPET) will be used to measure functional change in MVO2, RER, Exercise time, METs, and vitals.
Time frame: Cardiac hospitalizations or transplantation at 1 year.
Hospitalization for cardiac reasons or heart transplantation
Time frame: Number of deaths at 1 year
Number of patients who died during the study from all causes
Time frame: Change from baseline of serum biomarkers at 1-year
Serum inflammatory markers will be measured using ELISA assays (R&D systems) to test for change in inflammatory response. Biomarkers tested include IL6, TNF-alpha, GDF-15, and IL10. All biomarkers will be measured in pg/mL. All The biomarkers will be used predictively with clinical changes to assess correlation.
Time frame: Change from baseline of neuropsychological testing at 1-year
NIH toolbox Cognitive battery (for ages 7-85) will be used to evaluate change in neuropsychological function. These tests include:
Picture Vocabulary Test Oral Reading Recognition List Sorting Working Memory Test Pattern Comparison Processing Speed Test Picture Sequence Memory Test Flanker Inhibitory Control and Attention Test Dimensional Change Card Sort Test
The Cognition Battery produces three composite scores. A score of 100 is average
(the above description of tests is directly extracted from https://www.nihtoolbox.org)
Time frame: Change from baseline of NYHA Class at 1-year.
Subjective perception of functional capacity with NYHA Class I patients reporting no symptoms with exercise and rest to NYHA Class IV patients reporting symptoms at rest.
Time frame: Change from baseline of PROMIS composite score at 1 year
PROMIS measures patient-reported outcomes (PROs), such as pain, fatigue, physical functioning, emotional distress, and social role participation that have a major impact on quality-of-life across a variety of chronic diseases. PROMIS scores have a mean of 50 and standard deviation (SD) of 10 in a referent population. Scores 0.5 - 1.0 SD worse than the mean = mild symptoms/impairment Scores 1.0 - 2.0 SD worse than the mean = moderate symptoms/impairment, Scores 2.0 SD or more worse than the mean = severe symptoms/impairment
(information directly extracted from https://sphsoutcomes.net/promis-scoring)
Time frame: Change from baseline of KCCQ score at 1 year
The responses are categorized under 3 subscales (symptom burden, physical limitation and quality of life) with a range of possible subscale scores from 0 to 100, with 100 representing the least burden of symptoms. The total KCCQ score represents the mean of the three subscale scores.
(Extracted from https://www.ncbi.nlm.nih.gov)
Time frame: Change from baseline of Neuro-QOL score at 1 year
Neuro-QoL measures quantify the physical, mental, and social effects experienced by adults and children living with neurological conditions. Function scales, the range of responses is 0 to 4, with 0 being the worst possible total score and 80 being the best.
Contact information is provided by the study sponsor or research team.
Anita Saraf
Other
Acronym: EmpaCHD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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